@article{bb605962aa69445b8f80d00264247936,
title = "Sj{\"o}gren-like lacrimal Keratoconjunctivitis in germ-free mice",
abstract = "Commensal bacteria play an important role in the formation of the immune system but their role in the maintenance of immune homeostasis at the ocular surface and lacrimal gland remains poorly understood. This study investigated the eye and lacrimal gland phenotype in germ-free and conventional C57BL/6J mice. Our results showed that germ-free mice had significantly greater corneal barrier disruption, greater goblet cell loss, and greater total inflammatory cell and CD4+ T cell infiltration within the lacrimal gland compared to the conventionally housed group. A greater frequency of CD4+IFN-γ+ cells was observed in germ-free lacrimal glands. Females exhibited a more severe phenotype compared to males. Adoptive transfer of CD4+ T cells isolated from female germ-free mice into RAG1KO mice transferred Sj{\"o}gren-like lacrimal keratoconjunctivitis. Fecal microbiota transplant from conventional mice reverted dry eye phenotype in germ-free mice and decreased CD4+IFN-γ+ cells to levels similar to conventional C57BL/6J mice. These findings indicate that germ-free mice have a spontaneous lacrimal keratoconjunctivitis similar to that observed in Sj{\"o}gren syndrome patients and demonstrate that commensal bacteria function in maintaining immune homeostasis on the ocular surface. Thus, manipulation of intestinal commensal bacteria has the potential to become a novel therapeutic approach to treat Sj{\"o}gren Syndrome.",
keywords = "Commensal bacteria, Dry eye, Fecal transplant, Germ-free mice, Goblet cell, Sj{\"o}gren syndrome",
author = "Changjun Wang and Mahira Zaheer and Fang Bian and Darin Quach and Swennes, {Alton G.} and Britton, {Robert A.} and Pflugfelder, {Stephen C.} and {De Paiva}, {Cintia S.}",
note = "Funding Information: Acknowledgments: This work was supported by the NIH/NEY EY026893 (CSDP), Alkek Center for Metagenomics and Microbiome Research (CSDP), Biology of Inflammation Center (SCP and CSDP), NIH Training Grant T32-AI053831 (FB), RPB Stein Innovation Award (RAB), RPB Research to Prevent Blindness (SCP), The Oshman Foundation (SCP), William Stamps Farish Fund (SCP), The Hamill Foundation (SCP), Sid W. Richardson Foundation (SCP, CSDP), and by the Cytometry and Cell Sorting Core at Baylor College of Medicine, which is funded by the NIH NIAID P30AI036211, NCI P30CA125123, and NCRR S10RR024574, Zhejiang Provincial Medical and Health Science and Technology Program 2015KYA113 (CW), Zhejiang Key Laboratory Fund of China No. 2011E10006 (CW). We would like to thank Leiqi Zhang, Stephanie Fowler, Cynthia Pena-Olivo and Adam Cole for their expert assistance breeding and caring for conventional and germ-free mice. Funding Information: This work was supported by the NIH/NEY EY026893 (CSDP), Alkek Center for Metagenomics and Microbiome Research (CSDP), Biology of Inflammation Center (SCP and CSDP), NIH Training Grant T32-AI053831 (FB), RPB Stein Innovation Award (RAB), RPB Research to Prevent Blindness (SCP), The Oshman Foundation (SCP), William Stamps Farish Fund (SCP), The Hamill Foundation (SCP), Sid W. Richardson Foundation (SCP, CSDP), and by the Cytometry and Cell Sorting Core at Baylor College of Medicine, which is funded by the NIH NIAID P30AI036211, NCI P30CA125123, and NCRR S10RR024574, Zhejiang Provincial Medical and Health Science and Technology Program 2015KYA113 (CW), Zhejiang Key Laboratory Fund of China No. 2011E10006 (CW). We would like to thank Leiqi Zhang, Stephanie Fowler, Cynthia Pena-Olivo and Adam Cole for their expert assistance breeding and caring for conventional and germ-free mice. Publisher Copyright: {\textcopyright} 2018 by the authors. Licensee MDPI, Basel, Switzerland.",
year = "2018",
month = feb,
day = "13",
doi = "10.3390/ijms19020565",
language = "English",
volume = "19",
journal = "International journal of molecular sciences",
issn = "1661-6596",
number = "2",
}